Literature DB >> 9862477

Efficient initiation of S-phase in yeast requires Cdc40p, a protein involved in pre-mRNA splicing.

E Boger-Nadjar1, N Vaisman, S Ben-Yehuda, Y Kassir, M Kupiec.   

Abstract

The S. cerevisiae CDC40 gene was originally identified as a cell-division-specific gene that is essential only at elevated temperatures. Cells carrying mutations in this gene arrest with a large bud and a single nucleus with duplicated DNA content. Cdc40p is also required for spindle establishment or maintenance. Sequence analysis reveals that CDC40 is identical to PRP17, a gene involved in pre-mRNA splicing. In this paper, we show that Cdc40p is required at all temperatures for efficient entry into S-phase and that cell cycle arrest associated with cdc40 mutations is independent of all the known checkpoint mechanisms. Using immunofluorescence, we show that Cdc40p is localized to the nuclear membrane, weakly associated with the nuclear pore. Our results point to a link between cell cycle progression, pre-mRNA splicing, and mRNA export.

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Year:  1998        PMID: 9862477     DOI: 10.1007/s004380050891

Source DB:  PubMed          Journal:  Mol Gen Genet        ISSN: 0026-8925


  14 in total

1.  The carboxy terminal WD domain of the pre-mRNA splicing factor Prp17p is critical for function.

Authors:  L A Lindsey-Boltz; G Chawla; N Srinivasan; U Vijayraghavan; M A Garcia-Blanco
Journal:  RNA       Date:  2000-09       Impact factor: 4.942

Review 2.  The function of spliceosome components in open mitosis.

Authors:  Jennifer C Hofmann; Alma Husedzinovic; Oliver J Gruss
Journal:  Nucleus       Date:  2010-08-13       Impact factor: 4.197

3.  Extensive genetic interactions between PRP8 and PRP17/CDC40, two yeast genes involved in pre-mRNA splicing and cell cycle progression.

Authors:  S Ben-Yehuda; C S Russell; I Dix; J D Beggs; M Kupiec
Journal:  Genetics       Date:  2000-01       Impact factor: 4.562

4.  Functional analyses of interacting factors involved in both pre-mRNA splicing and cell cycle progression in Saccharomyces cerevisiae.

Authors:  C S Russell; S Ben-Yehuda; I Dix; M Kupiec; J D Beggs
Journal:  RNA       Date:  2000-11       Impact factor: 4.942

5.  Genetic and physical interactions between factors involved in both cell cycle progression and pre-mRNA splicing in Saccharomyces cerevisiae.

Authors:  S Ben-Yehuda; I Dix; C S Russell; M McGarvey; J D Beggs; M Kupiec
Journal:  Genetics       Date:  2000-12       Impact factor: 4.562

6.  A role for the yeast cell cycle/splicing factor Cdc40 in the G1/S transition.

Authors:  Yosef Kaplan; Martin Kupiec
Journal:  Curr Genet       Date:  2006-12-14       Impact factor: 3.886

7.  The functional study of human proteins using humanized yeast.

Authors:  Seho Kim; Juhee Park; Taekyung Kim; Jung-Shin Lee
Journal:  J Microbiol       Date:  2020-04-27       Impact factor: 3.422

8.  Mutations in genes of Saccharomyces cerevisiae encoding pre-mRNA splicing factors cause cell cycle arrest through activation of the spindle checkpoint.

Authors:  Orna Dahan; Martin Kupiec
Journal:  Nucleic Acids Res       Date:  2002-10-15       Impact factor: 16.971

9.  Drosophila MFAP1 is required for pre-mRNA processing and G2/M progression.

Authors:  Ditte S Andersen; Nicolas Tapon
Journal:  J Biol Chem       Date:  2008-09-02       Impact factor: 5.157

10.  The Saccharomyces cerevisiae gene CDC40/PRP17 controls cell cycle progression through splicing of the ANC1 gene.

Authors:  Orna Dahan; Martin Kupiec
Journal:  Nucleic Acids Res       Date:  2004-05-07       Impact factor: 16.971

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